HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 6-fluoro-1H-indole-5-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 6-fluoro-1-(triisopropylsilyl)-1H-indole-5-carboxylic acid | HCID 11559089 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 6-fluoro-1H-indole-5-carboxylic acid | HCID 11492033 | 103.5% |
Reaction Steps
6-Fluoro-1-(triisopropylsilyl)-1H-indole-5-carboxylic acid (4.36 g, 13.00 mmol) was treated with THF (30 mL) and tetra-n-butylammonium fluoride (1.0 M in THF, 13.0 mL, 13.00 mmol) and stirred at RT for 15 min. The reaction mixture was diluted with Et2O (30 mL) resulting in a suspension which was collected by filtration affording 6-fluoro-1H-indole-5-carboxylic acid (2.41 g) as a white crystalline solid. MS (ESI, pos. ion) m/z: 180.1 (M+H)+. The crude material was used in the subsequent reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321756B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-ebb4d035a7aa40af94828a1b9818ea92 |
| Source note | uspto-grants-2016_04 |